Evidence map›Paper›PMID 42374298›Full record

ArticleBMC pediatrics2026

The rationality of drug treatment and clinical characteristics in children with SARS-CoV-2 infection: a retrospective analysis.

Ling Su, Huo-Shu Chen, Wen-Liu Qiu, Wei-Min Zhong, Min Ren, Wen-Qiong He

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Article in BMC pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ling Su *The Fifth Hospital of Xiamen, Xiamen, 361101, China.
Huo-Shu Chen *The Fifth Hospital of Xiamen, Xiamen, 361101, China.
Wen-Liu QiuThe Fifth Hospital of Xiamen, Xiamen, 361101, China.
Wei-Min ZhongThe Fifth Hospital of Xiamen, Xiamen, 361101, China.
Min RenThe Fifth Hospital of Xiamen, Xiamen, 361101, China. renmin2022@qq.com.
Wen-Qiong HeThe Fifth Hospital of Xiamen, Xiamen, 361101, China. 19725042260@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWith the ongoing global pandemic of coronavirus disease 2019 (COVID-19), the rational use of medications and clinical profiles in the afflicted children-a particularly susceptible group-warrant further investigation. This paper analyzed the rationality of medicinal treatments and clinical characteristics in children with COVID-19.

methodsWe retrospectively reviewed the clinical data of pediatric inpatients with COVID-19 admitted to the Fifth Hospital of Xiamen from January 2025 to December 2025. Clinical classifications, symptoms, outcomes, complications and the use of therapeutic drugs were statistically analyzed. The rationality of medication was assessed by indication consistency and administration routes.

resultsThe clinical cure and improvement rate reached 99.22% in the 129 confirmed pediatric cases of COVID-19. They were categorized into a mild group (69 cases, 53.49%), a moderate group (59 cases, 45.74%), and a critical group (1 case, 0.77%). Clinical manifestations mainly included fever, cough, and runny nose. A significant difference was evident between the mild group and the moderate group in age, weight, outcomes, and clinical symptoms (e.g., coughing, runny nose, and nasal congestion) (P < 0.05 for all). Compared with the mild group, the moderate group reported a significantly higher reception of expectorants, nebulized inhalation medication, antihistamines, glucocorticoids, and antibiotics (P < 0.05 for all). In the mild and moderate groups, the irrational use of medications involved 3 types of drugs in 15 pediatric patients, including 2 cases (3.39%) of inhaled corticosteroid (ICS), 8 cases (13.11%) of antibacterial drugs, and 5 cases (5.43%) of interferon alpha 1b for injection. The irrationality of the first two types was attributed to inconsistent medication indications and that of the last type to mismatched administration routes. One rare complication, specifically multisystem inflammatory syndrome in children (MIS-C), was identified in the critical group.

conclusionThe clinical manifestations of COVID-19 in children are predominantly mild and moderate, with an overall favorable prognosis. The moderate group presents more pronounced respiratory symptoms (cough, runny nose, nasal congestion). The risk of complications in children with mild to moderate symptoms is similar, emphasizing the importance of early screening and prevention of complications. In clinical care for children with COVID-19, medication irrationality, such as indication inconsistency and mismatched administration routes, still exist in the administration of antiviral drugs, glucocorticoids, and antibiotics in some children with mild to moderate symptoms. The findings indicate a need for further optimizing real-world clinical practice and provide some insights for rational drug use.

Indexed as

COVID-19COVID-19 Drug TreatmentAdolescentAntiviral AgentsChildChild, PreschoolFemaleHumansInfantMaleRetrospective StudiesSARS-CoV-2Antiviral AgentsChildrenClinical featuresCOVID-19Drug treatmentSARS-CoV-2

Identifiers

PMID42374298
PMCPMC13595685

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.